Mitofilin complexes: conserved organizers of mitochondrial membrane architecture

作者：Zerbes Ralf M; van der Klei Ida J; Veenhuis Marten; Pfanner Nikolaus; van der Laan Martin^*; Bohnert Maria

来源：Biological Chemistry, 2012, 393(11): 1247-1261.

DOI：10.1515/hsz-2012-0239

• cristae
• crista junction
• Fcj1
• MINOS
• Mio10
• mitochondrial morphology

Mitofilin proteins are crucial organizers of mitochondrial architecture. They are located in the inner mitochondrial membrane and interact with several protein complexes of the outer membrane, thereby generating contact sites between the two membrane systems of mitochondria. Within the inner membrane, mitofilins are part of hetero-oligomeric protein complexes that have been termed the mitochondrial inner membrane organizing system (MINOS). MINOS integrity is required for the maintenance of the characteristic morphology of the inner mitochondrial membrane, with an inner boundary region closely apposed to the outer membrane and cristae membranes, which form large tubular invaginations that protrude into the mitochondrial matrix and harbor the enzyme complexes of the oxidative phosphorylation machinery. MINOS deficiency comes along with a loss of crista junction structures and the detachment of cristae from the inner boundary membrane. MINOS has been conserved in evolution from unicellular eukaryotes to humans, where alterations of MINOS subunits are associated with multiple pathological conditions.

• 出版日期2012-11